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Gafchromic™

FDA UDI

Class I (US FDA UDI)

by Ashland Specialty Ingredients, G.P.

Identity

Trade Name
Gafchromic™ FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, test object FDA UDI
Model / Reference
QuiCk Phantom w/EBT3P FDA UDI

Identifiers

Catalog Number
980672 FDA UDI
Primary DI / UDI-DI
00810106410357 FDA UDI
FDA Product Code
IXG FDA UDI
GMDN Term
Multi-modality therapeutic radiation phantom, test object FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1950 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-modality therapeutic radiation phantom, test object

Gafchromic™ by Ashland Specialty Ingredients, G.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, test object.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20cc31d4-6bae-4e28-8eb2-ee413448df55 33 fields · synced Jun 9, 2026